Welcome to LookChem.com Sign In|Join Free
  • or
2,3,5,6-Tetrafluorobis(phenylsulphonyl)benzene is a complex organic compound characterized by its unique molecular structure. It features a central benzene ring with fluorine atoms at the 2, 3, 5, and 6 positions, which imparts specific chemical properties due to the electronegativity of fluorine. Attached to this central ring are two phenylsulphonyl groups, which are benzene rings with a sulphonyl (-SO2-) group attached. 2,3,5,6-Tetrafluorobis(phenylsulphonyl)benzene is known for its thermal stability and is used in various chemical applications, including the synthesis of pharmaceuticals and other specialty chemicals. Its structure provides it with unique reactivity and selectivity in chemical reactions, making it a valuable intermediate in organic synthesis.

3851-64-7

Post Buying Request

3851-64-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3851-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3851-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,5 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3851-64:
(6*3)+(5*8)+(4*5)+(3*1)+(2*6)+(1*4)=97
97 % 10 = 7
So 3851-64-7 is a valid CAS Registry Number.

3851-64-7Downstream Products

3851-64-7Relevant academic research and scientific papers

LADDER POLYMERS WITH INTRINSIC MICROPOROSITY AND PROCESS FOR PRODUCTION THEREOF

-

Page/Page column 15-16, (2010/05/14)

A polymer of formula (I): where: n is an integer from 10 to 5,000; m is an integer from 10 to 5,000; Ar1 and Ar3 are the same or different and are residues derived from a tetra-hydroxy aromatic monomer, the tetra-hydroxy aromatic monomer being wherein R i

REACTION OF PERFLUOROARYL HALIDES WITH REDUCED SPECIES OF SULFUR DIOXIDE (HSO2(-), SO2(2-), S2O4(2-))

Grady, B. J.,Dittmer, D. C.

, p. 151 - 172 (2007/10/02)

Rongalite (sodium hydroxymethanesulfinate), sodium dithionite, and aminoiminomethanesulfinic acid (AIMS) reduce perfluoroiodobenzene in N,N-dimethylformamide to pentafluorobenzene.In the presence of added D2O or CH3OD, deuteriopentafluorobenzene is formed. p-Dinitrobenzene does not inhibit the reduction, and addition of norbonene did not result in trapping of any radical intermediates.Reaction of pentafluoroiodobenzene with sodium benzenesulfinate gave 1,4-dibenzenesulfonyl-2,3,5,6-tetrafluorobenzene.A halophilic attack mechanism is suggested for the reduction reaction.Chloropentafluorobenzene did not react under the same conditions as the iodide; at elevated temperatures in the presence of sodium bicarbonate and Rongalite the fluorine para to the chlorine was reduced.Reduction of the chloride to pentafluorobenzene is minor.In the absence of bicarbonate, the chloride gave also a mixture of sulfides believed to be derived from decomposition of the Rongalite to hydrogen sulfide.Some reaction with dimethylamine from decomposition of DMF also is observed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3851-64-7